EP0051558B1 - Dérivés de la prostacycline, leur préparation et leur utilisation dans des médicaments - Google Patents

Dérivés de la prostacycline, leur préparation et leur utilisation dans des médicaments Download PDF

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Publication number
EP0051558B1
EP0051558B1 EP81730114A EP81730114A EP0051558B1 EP 0051558 B1 EP0051558 B1 EP 0051558B1 EP 81730114 A EP81730114 A EP 81730114A EP 81730114 A EP81730114 A EP 81730114A EP 0051558 B1 EP0051558 B1 EP 0051558B1
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Prior art keywords
group
optionally
carbon atoms
benzoyloxy
general formula
Prior art date
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Expired
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EP81730114A
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German (de)
English (en)
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EP0051558A1 (fr
Inventor
Werner Dr. Skuballa
Helmut Prof. Vorbrüggen
Bernd Dr. Radüchel
Olaf Dr. Loge
Peter Dr. Vischer
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Bayer Pharma AG
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Schering AG
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Priority to AT81730114T priority Critical patent/ATE6861T1/de
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/93—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems condensed with a ring other than six-membered
    • C07D307/935—Not further condensed cyclopenta [b] furans or hydrogenated cyclopenta [b] furans
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/08—Bronchodilators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/08—Vasodilators for multiple indications
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/93—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems condensed with a ring other than six-membered
    • C07D307/935—Not further condensed cyclopenta [b] furans or hydrogenated cyclopenta [b] furans
    • C07D307/937—Not further condensed cyclopenta [b] furans or hydrogenated cyclopenta [b] furans with hydrocarbon or substituted hydrocarbon radicals directly attached in position 2, e.g. prostacyclins
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804—Compounds having Si-O-C linkages

Definitions

  • the invention relates to new prostacyclin derivatives, processes for their preparation and their use as medicaments.
  • Prostacyclin (PGl 2 ), one of the main factors in platelet aggregation, has a dilating effect on various blood vessels (Science 196, 1072) and could therefore be considered as a means of lowering blood pressure.
  • PGl 2 does not have the stability necessary for a drug. Its half-life is only a few minutes at physiological pH values and at room temperature.
  • DE-OS 27 53 244 describes prostacyclin derivatives which are stabilized by a nitrile group on the enol ether double bond.
  • the compounds according to the invention have a vasodilating, hypotensive and bronchodilatory effect. They are also suitable for inhibiting platelet aggregation and gastric acid secretion.
  • the hydroxyl groups R 1 and in W can be functionally modified, for example by etherification or esterification, it being possible for the free or modified hydroxyl groups in W to be a- or ⁇ -permanent, with free hydroxyl groups being preferred.
  • the radicals known to the person skilled in the art are suitable as ether and acyl radicals. Easily removable ether residues such as, for example, the tetrahydropyranyl, tetrahydrofuranyl, a-ethoxyethyl, trimethylsilyl, dimethyl-tert-butylsilyl and tribenzylsilyl residue are preferred.
  • Suitable acyl radicals are C 1 -C 4 -alkanoyl radicals such as acetyl, propionyl, butyryl or benzoyl.
  • R 2 are straight-chain and branched-chain, saturated and unsaturated alkyl radicals having 1-7 C atoms or the phenyl group.
  • Suitable alkylene group D are straight-chain or branched-chain saturated alkylene radicals having 1-5 C atoms, which may be substituted by fluorine atoms. Examples include: methylene, fluoromethylene, ethylene, 1,2-propylene, ethylethylene, trimethylene, tetramethylene, pentamethylene, 1-methyl-tetramethylene, 1-methyl-trimethylene, 2-methyltrimethylene, 2-methyl-tetramethylene.
  • alkylene group B Straight-chain or branched-chain alkylene radicals with 1-5 C atoms are suitable as alkylene group B. Examples include: methylene, ethylene, trimethylene, tetramethylene and pentamethylene.
  • the invention further relates to a process for the preparation of the prostacyclin derivatives of the general formula I according to the invention, characterized in that a compound of the general formula II wherein R i , R 2 , A, W, D, E have the meanings given above, optionally after protecting free hydroxyl groups present after reaction with a carbanion prepared from the nitrile of the general formula III and lithium diisopropylamide, where R 3 is an easily removable ether radical means and B has the meaning given above, is subjected to an acid treatment.
  • Suitable ether radicals R 3 in the compound of the general formula III are the radicals familiar to the person skilled in the art. Easily removable ether residues such as, for example, dimethyl-tert-butyl-silyl, trimethylsilyl, tribenzylsilyl, tetrahydropyranyl, tetrahydrofuranyl and a-ethoxyethyl are preferred, to name just a few.
  • the reaction of the compound of general formula II (preparation analogous to DE-OS 28 45 770) with the organometallic compound of general formula 111, which is prepared from the corresponding nitrile with lithium diisopropylamide in ether / tetrahydrofuran mixtures in the presence of hexamethylphosphoric triamide, is carried out at temperatures of 0 to -100 ° C, preferably at - 60 to - 78 ° C, in a solvent or solvent mixture suitable for organometallic reactions, preferably diethyl ether or tetrahydrofuran.
  • the crude product of the organometallic reaction is treated with a catalytic amount of an acid in a water-immiscible solvent, such as toluene, benzene, methylene chloride, chloroform, carbon tetrachloride or diethyl ether, preferably in toluene or diethyl ether at temperatures between
  • Suitable acids are p-toluenesulfonic acid, sulfuric acid, hydrochloric acid or boron trifluoride.
  • the functional modification of the free OH groups takes place according to the methods known to the person skilled in the art.
  • reaction is carried out, for example, with dihydropyran in methylene chloride, benzene or chloroform using an acidic catalyst, such as POC1 3 , p-toluenesulfonic acid or anhydrous mineral acids.
  • the dihydropyran is used in excess, preferably in 2 to 10 times the theoretical amount.
  • the reaction is usually complete at 0 to 30 ° C after 15 to 30 minutes.
  • the acyl protective group is introduced by reacting a compound of the general formula I in a manner known per se with a carboxylic acid derivative, such as, for example, acid chloride or acid anhydride in the presence of a tertiary amine base, e.g. Reacts pyridine or dimethylaminopyridine.
  • a carboxylic acid derivative such as, for example, acid chloride or acid anhydride
  • a tertiary amine base e.g. Reacts pyridine or dimethylaminopyridine.
  • a functionally modified OH group is released to the compounds of the general formula by known methods.
  • the cleavage of the ether protecting group is carried out in an aqueous solution of an organic acid such as acetic acid or propionic acid or in an aqueous solution of an inorganic acid such as e.g. Hydrochloric acid.
  • an organic acid such as acetic acid or propionic acid
  • an inorganic acid such as e.g. Hydrochloric acid.
  • a water-miscible inert organic solvent is expediently added.
  • Suitable organic solvents are, for example, alcohols, such as methanol and ethanol, and ethers, such as dimethoxyethane, dioxane and tetrahydrofuran. Tetrahydrofuran is preferred.
  • the cleavage is preferably carried out at temperatures between 20 and 80 ° C.
  • the silyl ether protective group is split off, for example, with tetrabutylammmonium fluoride or with KF in the presence of a crown ether.
  • Suitable solvents are, for example, tetrahydrofuran, diethyl ether, dioxane or methylene chloride.
  • the cleavage is preferably carried out at temperatures between 0 and 80 ° C.
  • the acyl group is saponified, for example, with alkali or alkaline earth carbonates or hydroxides in an alcohol or in the aqueous solution of an alcohol.
  • Aliphatic alcohols such as, for example, methanol, ethanol or butanol, preferably methanol, are suitable as alcohols.
  • Potassium and sodium salts may be mentioned as alkali carbonates and hydroxides, but the potassium salts are preferred.
  • Suitable alkaline earth carbonates and hydroxides are, for example, calcium carbonate, calcium hydroxide and barium carbonate. The reaction takes place at -10 to 70 ° C, preferably at 25 ° C.
  • the nitriles of the general formula 1 thus prepared are mixtures of isomers which can be separated by customary separation methods, such as, for example, column chromatography or layer chromatography.
  • nitriles of the general formula III used for the process can be prepared, for example, from 1,5-alkanediols by selective silylation, tosylation and subsequent reaction with sodium or potassium cyanide.
  • the compounds of this invention are hypotensive and bronchodilatory. They are also suitable for inhibiting platelet aggregation.
  • the new prostacyclin derivatives of the general formula I are valuable pharmaceutical active ingredients.
  • they have a higher specificity and, above all, a substantially longer activity.
  • PG1 2 they are characterized by greater stability.
  • the high tissue specificity of the new prostaglandins can be seen when examining smooth muscle organs, such as the guinea pig ileum or the isolated rabbit trachea, where a significantly lower stimulation can be observed than when applying natural prostaglandins of the E, A or F type.
  • the new prostaglandin analogues have the properties typical of prostacyclins, such as lowering of the peripheral arterial and coro naren vascular resistance, inhibition of platelet aggregation and dissolution of platelet thrombi, myocardial cytoprotection and thus lowering of systemic blood pressure without simultaneously reducing stroke volume and coronary blood flow; Treatment of stroke, prophylaxis and therapy of coronary heart diseases, coronary thrombosis, heart attack, peripheral arterial diseases, arteriosclerosis and thrombosis, therapy of shock, inhibition of bronchoconstriction, inhibition of gastric acid secretion and cytoprotection of the gastric and intestinal mucosa; Cytoprotection on the pancreas, anti-allergic properties, reduction of pulmonary vascular resistance and blood pressure, promotion of renal blood flow, use instead of heparin or as an adjuvant for dialysis of hemofiltration, preservation of blood plasma preserves, especially before preserving blood platelets, inhibition of birth defects, treatment of birth defects , Increased cerebral
  • the dose of the compounds is 1-1500 ⁇ g / kg / day when administered to the human patient.
  • the unit dose for the pharmaceutically acceptable carrier is 0.01-100 mg.
  • the compounds according to the invention show a greater hypotensive and longer-lasting effect than PGE 2 and PGA 2 without triggering cardiac arrhythmias like PGE 2 diarrhea or PGA 2 .
  • the compounds according to the invention When injected intensively into anesthetized rabbits, the compounds according to the invention show a stronger and considerably longer lasting reduction in blood pressure compared to PGE 2 and PGA 2 , without affecting other smooth-muscular organs or organ functions.
  • Sterile, injectable, aqueous or oily solutions are used for parenteral administration.
  • Tablets, coated tablets or capsules, for example, are suitable for oral administration.
  • the invention thus also relates to medicaments based on the compounds of the general formula I and customary auxiliaries and carriers.
  • the active compounds according to the invention are to be used in conjunction with the auxiliaries known and customary in galenics, e.g. serve to manufacture blood pressure lowerers.
  • reaction product of the reaction described above is dissolved in 150 ml of abs. Diethyl ether, adds 90 ml of a dilute ethereal boron trifluoride solution (preparation: 0.9 ml of 45% boron trifluoride etherate solution is diluted with 81 ml of absolute ether) and stirred for 1 hour at room temperature under argon. Then poured onto 5% sodium bicarbonate solution, washed neutral with water, dried over sodium sulfate and evaporated in vacuo.
  • the 1.2 g of the (5E) -configured compound are stirred for 18 hours at room temperature with 40 ml of a mixture of glacial acetic acid / water / tetrahydrofuran (65 + 35 + 10). It is evaporated in vacuo and the residue is chromatographed on silica gel. With methylene chloride / isopropanol (9 + 1), 740 mg of the title compound is obtained as a colorless oil.
  • IR 3610, 3400 (wide), 2960, 2930, 2860, 2200,1650,1600,970 / cm.
  • IR 2960, 2925, 1770, 1715, 1602, 1585, 1270.969 / cm.
  • tosylate To form tosylate, dissolve in 185 ml of pyridine and add 74 g of p-toluenesulfonic acid chloride at an ice bath temperature. The mixture is stirred for 16 hours at room temperature, mixed with 10 ml of water, stirred for 3 hours, diluted with 1.3 liters of ether, shaken twice with 10% sulfuric acid, once with 5% sodium bicarbonate solution and three times with water. It is dried over magnesium sulfate and evaporated in vacuo. This gives 79 g of tosylate, which is dissolved in 185 ml of dimethyl sulfoxide, mixed with 22 g of sodium cyanide and stirred at 80 ° C. under argon for 18 hours.
  • IR 2930, 2855, 2242, 1250, 1095, 830 / cm.
  • reaction product of the reaction described above is dissolved in 120 ml of abs. Diethyl ether, adds 60 ml of a dilute ethereal boron trifluoride solution (preparation: Example 1) and stirred for 1 hour at room temperature. Then poured onto 5% sodium bicarbonate solution, washed with; Water neutral, dries over magnesium sulfate and evaporates in vacuo.
  • IR 3600, 3400, 2930, 2860, 2198, 1650, 1599, 1586, 970 cm.
  • IR 2940, 1770, 1714, 1599, 1586, 1270, 970 / cm.
  • IR 3600, 3400, 2962, 2935, 2860, 2200, 1650, 1600.972 / cm.
  • Example 1 a Analogously to Example 1 a, 1.6 g of (1 S, 5R, 6R, 7R) -6 - [(E) - (3R) -3-hydroxy-4,4-dimethyl-1-octenyl] - 7-benzoyloxy-2-oxybicyclo [3.3.0] octan-3-one, 8 ml pyridine and 1 ml benzoyl chloride 2 g of the dibenzoate as a colorless oil.
  • IR 2962, 2930, 1770, 1715, 1600, 1588, 1270.970 / cm.
  • IR 3600, 3400 (wide), 2965, 2935, 2863, 2200, 1650, 1602.972 / cm.
  • IR 3610, 3420, 2960, 2935, 2863, 2200, 1650, 1600, 970 / cm.
  • IR 2960, 2935, 1771, 1715, 1600, 1589, 1270.972 / cm.
  • IR 3630, 3410, 2958, 2936, 2860, 2202, 1650, 972 / cm.
  • IR 2958, 2930, 2840, 1768, 1716, 1600, 1590, 1272, 976 / cm.
  • IR 3605, 3430, 2960, 2936, 2200, 1650, 976 / cm.
  • IR 2960, 2932, 2845, 1765, 1712, 1600, 1588, 1270, 972 / cm.
  • IR 3600, 3410, 2958, 2934, 2200, 1652, 1602.974 / cm.
  • IR 2960, 2940, 2832, 1765, 1718, 1600, 1588, 1275, 974 / cm.
  • IR 3605, 3410, 2962, 2938, 2204, 1652, 1600.1588 / cm.
  • IR 2960, 2938, 1766, 1716, 1600, 1590, 1270 / cm.
  • IR 3600, 3420, 2956, 2934, 2840, 2202, 1650, 976 / cm.
  • IR 2960, 2935, 1770, 1716, 1600, 1588, 1274.976 / cm.
  • IR 3605, 3400, 2930, 2865, 2210, 1650, 1600, 1588.976 / cm.
  • IR 3610, 3410, 2958, 2936, 2862, 2200, 1650, 1601.972 / cm.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Furan Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Claims (4)

1. Dérivés de la prostacycline qui répondent à la formule générale I:
Figure imgb0009
dans laquelle
B représente un radical alkylène, linéaire ou ramifié, contenant de 1 à 5 atomes de carbone,
A représente un radical -CH2-CH2-, un radical -CH=CH-trans ou un radical-C≡C-,
W représente un radical hydroxyméthylène libre ou sous la forme d'un dérivé fonctionnel ou un
Figure imgb0010
fonctionnel, le radical -OH ayant la configuration a ou la configuration β,
D et E forment ensemble une liaison directe ou
D représente un radical alkylène saturé, linéaire ou ramifié, qui contient de 1 à 5 atomes de carbone et qui peut porter des atomes de fluor,
E représente l'oxygène, une liaison -C≡C- ou une liaison directe,
R2 représente un radical alkyle en C1-C7 ou un radical phényle et
R1 représente un radical hydroxy libre ou sous la forme d'un dérivé fonctionnel.
2. Cyano-5 décarboxy-2 hydroxyméthyl-2 phénoxy-16 tétranor-17,18,19, 20 prostacycline-(5Z).
3. Procédé de préparation de dérivés de la prostacycline répondant à la formule générale (I), procédé caractérisé en ce qu'on fait réagir un composé répondant à la formule générale Il
Figure imgb0011
dans laquelle R1, R2, A, W, D et E ont les significations indiquées ci-dessus, avec un carbanion préparé à partir du diisopropylamidure de lithium et d'un nitrile répondant à la formule générale I II
Figure imgb0012
dans laquelle B a la signification précédemment donnée, puis on soumet le composé obtenu, le cas échéant après en avoir protégé les éventuels radicaux hydroxy libres, à un traitement par un acide.
4. Médicament contenant un ou plusieurs composés selon la revendication 1 ainsi que des adjuvants et excipients usuels.
EP81730114A 1980-10-31 1981-10-29 Dérivés de la prostacycline, leur préparation et leur utilisation dans des médicaments Expired EP0051558B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT81730114T ATE6861T1 (de) 1980-10-31 1981-10-29 Prostacyclinderivate, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19803041601 DE3041601A1 (de) 1980-10-31 1980-10-31 Neue prostacyclinderivate, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel
DE3041601 1980-10-31

Publications (2)

Publication Number Publication Date
EP0051558A1 EP0051558A1 (fr) 1982-05-12
EP0051558B1 true EP0051558B1 (fr) 1984-03-28

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EP81730114A Expired EP0051558B1 (fr) 1980-10-31 1981-10-29 Dérivés de la prostacycline, leur préparation et leur utilisation dans des médicaments

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US (1) US4364951A (fr)
EP (1) EP0051558B1 (fr)
JP (1) JPS57206679A (fr)
AT (1) ATE6861T1 (fr)
CA (1) CA1205467A (fr)
DE (2) DE3041601A1 (fr)
DK (1) DK159313C (fr)
HU (1) HU187466B (fr)
IE (1) IE52302B1 (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3322893A1 (de) * 1983-06-23 1985-01-03 Schering AG, 1000 Berlin und 4709 Bergkamen Neue prostacyclinderivate, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel
US4684624A (en) * 1983-12-22 1987-08-04 Yoshio Hosobuchi Method of treating cerebral ischemia
US4880939A (en) * 1986-12-11 1989-11-14 Toray Industries 2,5,6,7-tetranor-18,18,19,19-tetradehydro-4,8-inter-m-phenylene PGI2 derivatives
JPS63174984A (ja) * 1987-01-16 1988-07-19 Nissan Chem Ind Ltd シアノプロスタサイクリン類の合成法
AU6117398A (en) * 1997-02-27 1998-09-18 Toray Industries, Inc. Drugs for ameliorating pulmonary circulation
US6032956A (en) * 1999-03-05 2000-03-07 Bogucz; John Board game
EP1641462B1 (fr) * 2003-07-03 2010-11-24 Sucampo AG Composition entero-soluble comprenant des analogues de prostaglandine, utilisee comme agent d'ouverture des canaux a chlorure
EP1975163A1 (fr) * 2007-03-28 2008-10-01 Bayer Schering Pharma Aktiengesellschaft Nouveaux dérivés de 5-cyano-prostacycline et leur utilisation en tant qu'agents pour le traitement d'infection virale de la grippe
EP1988087A1 (fr) * 2007-03-28 2008-11-05 Bayer Schering Pharma Aktiengesellschaft Nouveaux dérivés de 5-cyano-prostacycline et leur utilisation en tant qu'agents pour le traitement de maladies auto-immunes
US20080242713A1 (en) * 2007-03-28 2008-10-02 Bayer Schering Pharma Aktiengesellschaft Novel 5-cyano-prostacyclin derivatives as agents for the treatment of autoimmune diseases
US7776896B2 (en) * 2007-03-28 2010-08-17 Bayer Schering Pharma Aktiengesellschaft 5-cyano-prostacyclin derivatives as agents for the treatment of influenza a viral infection

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2753244A1 (de) * 1977-11-25 1979-06-07 Schering Ag Neue prostacyclinderivate und verfahren zu ihrer herstellung

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JPH036146B2 (fr) 1991-01-29
DK159313B (da) 1990-10-01
IE812535L (en) 1982-04-30
EP0051558A1 (fr) 1982-05-12
DK159313C (da) 1991-02-25
HU187466B (en) 1986-01-28
CA1205467A (fr) 1986-06-03
DE3041601A1 (de) 1982-06-16
JPS57206679A (en) 1982-12-18
DE3162910D1 (en) 1984-05-03
US4364951A (en) 1982-12-21
DK480581A (da) 1982-05-01
ATE6861T1 (de) 1984-04-15
IE52302B1 (en) 1987-09-02

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